Warning letter
Polychrome Medical, Inc: warning letter of Dec 7, 2007
FDA warning letter UCM076592 · Minneapolis District Office
Key facts
| Reference number | UCM076592 |
|---|---|
| Company | Polychrome Medical, Inc |
| Subject | CGMP/QSR/Manufacture/Packing/Storage/Installation/Adulterated |
| Issue date | Dec 7, 2007 |
| Posted date | Dec 7, 2007 |
| Issuing office | Minneapolis District Office |
| Product type | Unknown |
| CFR sections cited | 820 |
| Country | 3 |
| Letter on fda.gov | web.archive.org |
At a glance
- 1–9 CFR sections cited
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA warning letters
FDA warning letters notify a firm of significant regulatory violations found during an inspection or review and request prompt corrective action.
Source: U.S. Food and Drug Administration (FDA), Warning Letters · Source date: